Smart crystalline framework materials with a triazole carboxylic acid ligand: fluorescence sensing and catalytic reduction of PNP†

IF 3.5 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR
Qiu Lv, Qing Lin Guan, Jin Long Li, Jin Xiao Li, Jing Jin, Feng Ying Bai and Yong Heng Xing
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Abstract

Triazole polycarboxylic acid ligands are widely employed in the construction of MOFs due to their strong coordination ability and flexible coordination modes. In this work, three novel complexes (Pb(MCTCA)(H2O) (1), Co(HMCTCA)2(H2O)2 (2) and Cu(HMCTCA)2(H2O)2 (3)) based on the H2MCTCA ligand (5-methyl-1-(4-carboxyl)-1H-1,2,3-triazole-4-carboxylic acid) were successfully synthesized under hydrothermal conditions, respectively. X-ray single crystal structure analysis shows that complex 1 is a 3D network structure, where the central metal Pb(II) is six coordinated to form deformed triangular prism geometry. The complexes 2 and 3 are both 2D layer supramolecular structures connected through intermolecular hydrogen, where the central metals (Co/Cu) are six coordinated to form octahedral configuration geometry. Based on functional properties, it is found that complex 1 exhibits excellent detection ability for small-molecule drugs (azithromycin, colchicine and balsalazide disodium) and actinide cations (Th4+ and UO22+) within a lower concentration range without interference from other components. In particular, the detection limits of three small-molecule drugs are all lower than 0.30 μM. In addition, complexes 2 and 3 exhibited excellent catalytic reduction performance toward p-nitrophenol (PNP), with a reduction efficiency exceeding 98%. These experimental results evidence that complexes 1–3 have potential application prospects in fluorescence sensing and catalytic reduction.

Abstract Image

具有三唑羧酸配体的智能晶体框架材料:PNP的荧光传感和催化还原。
三唑多羧酸配体因其较强的配位能力和灵活的配位模式而被广泛应用于MOFs的构建。本工作在水热条件下成功合成了三种基于H2MCTCA配体(5-甲基-1-(4-羧基)-1H-1,2,3-三唑-4-羧酸)的新型配合物(Pb(MCTCA)(H2O)(1)、Co(HMCTCA)2(H2O)2(2)和Cu(HMCTCA)2(H_2O)2(3))。X射线单晶结构分析表明,配合物1是一种三维网络结构,其中中心金属Pb(II)是六配位的,形成变形的三棱柱几何结构。配合物2和3都是通过分子间氢连接的2D层超分子结构,其中中心金属(Co/Cu)是六配位的,形成八面体构型几何形状。基于功能性质,发现配合物1在较低浓度范围内对小分子药物(阿奇霉素、秋水仙碱和巴柳氮二钠)和锕系阳离子(Th4+和UO22+)表现出优异的检测能力,而不会受到其他成分的干扰。特别是三种小分子药物的检测限均低于0.30μM。此外,配合物2和3对对对硝基苯酚(PNP)表现出优异的催化还原性能,还原效率超过98%。这些实验结果证明配合物1-3在荧光传感和催化还原方面具有潜在的应用前景。
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来源期刊
Dalton Transactions
Dalton Transactions 化学-无机化学与核化学
CiteScore
6.60
自引率
7.50%
发文量
1832
审稿时长
1.5 months
期刊介绍: Dalton Transactions is a journal for all areas of inorganic chemistry, which encompasses the organometallic, bioinorganic and materials chemistry of the elements, with applications including synthesis, catalysis, energy conversion/storage, electrical devices and medicine. Dalton Transactions welcomes high-quality, original submissions in all of these areas and more, where the advancement of knowledge in inorganic chemistry is significant.
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